Meloxicam Capsule 15 mg (Meloxicam)

Adult dose

1. Acute exacerbation of osteoarthritis (degenerative arthritis): ○ Adults: Administer meloxicam 7.5 mg orally once daily. If symptoms do not improve, the dose may be increased to 15 mg per day as needed. 2. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15 mg of this medicine orally once daily. The dose may be reduced to 7.5 mg per day depending on the response to treatment. Do not administer more than 15 mg per day. Take with water or another beverage during a meal. ○ In elderly patients or patients at increased risk of adverse reactions, treatment is usually initiated at 7.5 mg per day. ○ Patients with severe renal impairment receiving hemodialysis should not receive more than 7.5 mg per day.

This medication poses a risk of gastrointestinal bleeding in individuals who regularly consume more than three alcoholic beverages a day, so it is essential to consult a doctor or pharmacist. This medication can increase the risk of cardiovascular diseases, so caution is required for individuals with a history of heart disease or stroke, or those with risk factors. If symptoms such as chest pain, shortness of breath, weakness, or stuttering occur while taking this medication, it should be stopped immediately and medical assistance sought. As a nonsteroidal anti-inflammatory drug, this medication can cause serious gastrointestinal side effects such as bleeding, ulcers, and perforation; caution is especially needed for patients with a history of gastrointestinal disorders or the elderly. If discomfort or bleeding symptoms occur in the gastrointestinal tract during the course of treatment, the healthcare team should be informed immediately, and medication may be halted if necessary. This drug may cause severe skin reactions or allergic reactions; thus, it should be discontinued immediately if skin rash, mucosal damage, or difficulty breathing occurs. It can affect kidney function, so patients with kidney disease or those on diuretics or blood pressure medications should undergo regular kidney function tests. This medication can affect liver function, so those with liver disease or abnormal liver function test results should consult a doctor. Pregnant women or women who might become pregnant should not take this medication, and women planning a pregnancy should avoid it as well. It is also not recommended for breastfeeding women, and it should not be administered to children or adolescents under 15 years of age. Regular blood tests and liver and kidney function assessments should be conducted to check for abnormalities in individuals taking this medication for an extended period. Due to many potential drug interactions, it is vital to inform the doctor when taking it in combination with medications like aspirin, anticoagulants, diuretics, blood pressure medications, lithium, or methotrexate. As this medication may cause side effects such as drowsiness and dizziness, caution is advised when driving or operating machinery. In case of overdose, gastric lavage and general supportive care should be administered, as there is no specific antidote; therefore, medical attention should be sought immediately. This medication should be kept out of reach of children and stored sealed in its original container.

• Gastrointestinal bleeding
• cardiovascular thrombotic reactions
• myocardial infarction
• stroke
• bleeding from the stomach or intestines
• ulcers
• perforation
• exfoliative dermatitis
• Stevens-Johnson syndrome
• toxic epidermal necrolysis

This medication is sensitive to light and should be stored in a container that prevents light exposure. Additionally, it should be kept at a temperature between 1 and 30 degrees Celsius for optimal efficacy.

Appearance

A dark green capsule with a yellowish powder inside.

Package unit

30 capsules/bottle, 100 capsules/bottle